定向清除 PD-1 表达细胞,通过外周克隆删除诱导免疫耐受

IF 17.6 1区 医学 Q1 IMMUNOLOGY
Jikai Cui, Heng Xu, Jizhang Yu, Shuan Ran, Xi Zhang, Yuan Li, Zhang Chen, Yuqing Niu, Song Wang, Weicong Ye, Wenhao Chen, Jie Wu, Jiahong Xia
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引用次数: 0

摘要

胸腺负性选择 T 细胞受体(TCR)复合物对建立器官移植后的自身耐受性和获得性异体移植耐受性至关重要。然而,异体活性 T 细胞外周克隆性删除是否以及如何诱导移植耐受尚不清楚。在这里,我们发现程序性细胞死亡蛋白 1(PD-1)是异体活性 T 细胞的标志,与异体抗原相遇后的克隆扩增有关。此外,我们还发现,白喉毒素受体(DTR)介导的 PD-1+ 细胞消融可通过异体活性 T 细胞外周克隆性删除重塑 TCR 重排,并促进小鼠移植模型的耐受性。此外,通过使用 PD-1 特异性清除抗体,我们发现抗体介导的 PD-1+ 细胞清除可防止心脏移植排斥反应和人源化 PD-1 小鼠实验性自身免疫性脑脊髓炎(EAE)的发生。因此,这些数据表明,PD-1 是外周克隆清除和诱导免疫耐受的一个有吸引力的靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Targeted depletion of PD-1–expressing cells induces immune tolerance through peripheral clonal deletion
Thymic negative selection of the T cell receptor (TCR) repertoire is essential for establishing self-tolerance and acquired allograft tolerance following organ transplantation. However, it is unclear whether and how peripheral clonal deletion of alloreactive T cells induces transplantation tolerance. Here, we establish that programmed cell death protein 1 (PD-1) is a hallmark of alloreactive T cells and is associated with clonal expansion after alloantigen encounter. Moreover, we found that diphtheria toxin receptor (DTR)–mediated ablation of PD-1+ cells reshaped the TCR repertoire through peripheral clonal deletion of alloreactive T cells and promoted tolerance in mouse transplantation models. In addition, by using PD-1–specific depleting antibodies, we found that antibody-mediated depletion of PD-1+ cells prevented heart transplant rejection and the development of experimental autoimmune encephalomyelitis (EAE) in humanized PD-1 mice. Thus, these data suggest that PD-1 is an attractive target for peripheral clonal deletion and induction of immune tolerance.
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来源期刊
Science Immunology
Science Immunology Immunology and Microbiology-Immunology
CiteScore
32.90
自引率
2.00%
发文量
183
期刊介绍: Science Immunology is a peer-reviewed journal that publishes original research articles in the field of immunology. The journal encourages the submission of research findings from all areas of immunology, including studies on innate and adaptive immunity, immune cell development and differentiation, immunogenomics, systems immunology, structural immunology, antigen presentation, immunometabolism, and mucosal immunology. Additionally, the journal covers research on immune contributions to health and disease, such as host defense, inflammation, cancer immunology, autoimmunity, allergy, transplantation, and immunodeficiency. Science Immunology maintains the same high-quality standard as other journals in the Science family and aims to facilitate understanding of the immune system by showcasing innovative advances in immunology research from all organisms and model systems, including humans.
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